Welcome to our dedicated page for Vir Biotechnology news (Ticker: VIR), a resource for investors and traders seeking the latest updates and insights on Vir Biotechnology stock.
Vir Biotechnology, Inc. reports developments as a clinical-stage biopharmaceutical company developing medicines for serious infectious diseases and cancer. Recurring updates cover its chronic hepatitis delta program, including the investigational combination of tobevibart and elebsiran, and its oncology portfolio of PRO-XTEN® dual-masked T-cell engagers across solid tumor targets.
Company news also includes clinical data presentations, trial progress, financial results, equity financing activity, and strategic collaborations. Its VIR-5500 program is a PSMA-targeted PRO-XTEN® dual-masked T-cell engager for metastatic prostate cancer, and the company also describes preclinical work across infectious diseases and oncologic malignancies.
Vir Biotechnology, Inc. announced a $55 million initial investment from BARDA, with a total potential of $1 billion for pandemic preparedness. The company is advancing Phase 2 data for hepatitis B, D, and influenza A, expected in 2023. Financially, Vir reported Q3 revenues of $374.6 million, significantly up from $103.6 million in Q3 2021, driven by collaboration revenue from GSK related to sotrovimab. Vir maintains a strong balance sheet with approximately $2.7 billion in cash, supporting its innovative portfolio.
Vir Biotechnology announced acceptance of four abstracts for presentation at the AASLD The Liver Meeting from November 4-8, 2022, in Washington, D.C. Key highlights include new safety and efficacy data from the Phase 2 MARCH trial involving investigational treatments VIR-2218 (siRNA) and VIR-3434 (monoclonal antibody). Notably, results indicate significant reductions in HBV viral DNA and HBsAg levels. The meeting will feature two oral presentations, including one deemed 'late-breaking,' and two poster presentations, showcasing promising developments in HBV treatment aimed at achieving functional cures.
Vir Biotechnology (Nasdaq: VIR) will provide a corporate update and report its third-quarter financial results on November 3, 2022. These results cover the period ending September 30, 2022, and will be released after market close. Investors can access the update through the company’s website. Vir focuses on immunology and has a development pipeline targeting serious infectious diseases, including COVID-19 and hepatitis. The company combines immunologic insights with advanced technologies to enhance immune response.
Vir Biotechnology has initiated the Phase 2 PENINSULA trial, dosing the first participant with the investigational monoclonal antibody VIR-2482, aimed at preventing influenza A illness. Funded partly by a $55 million U.S. government grant, this trial will assess the efficacy and safety of two doses in about 3,000 healthy adults aged 18 to 64. Initial data is expected in mid-2023. VIR-2482 is designed to provide broad strain protection throughout a flu season and may address the current flu vaccine efficacy gap of around 40%.
Vir Biotechnology announced that Phil Pang, M.D., Ph.D., their executive vice president and chief medical officer, will present at the H. C. Wainwright 3rd Annual Hepatitis B Virus (HBV) Conference on October 18, 2022, at 10:30 a.m. PT / 1:30 p.m. ET. A live webcast of the presentation can be accessed on the Vir website and will be available for 30 days.
Vir focuses on immunology and has a pipeline targeting serious infectious diseases such as COVID-19 and hepatitis B.
Vir Biotechnology announces a multi-year contract with the Biomedical Advanced Research and Development Authority (BARDA), initially valued at $55 million, to develop VIR-2482, a monoclonal antibody for influenza. The contract has the potential to extend up to $1 billion for influenza and other infectious disease candidates. The Phase 2 trial for VIR-2482 is anticipated to start in late 2022, with initial data expected by mid-2023. This collaboration is aimed at enhancing public health responses to infectious disease threats.
On September 22, 2022, Vir Biotechnology announced the dosing of the first patient in the Phase 2 SOLSTICE trial aimed at treating chronic hepatitis D virus (HDV) infection. This trial evaluates the efficacy of VIR-2218 and VIR-3434, a combination strategy designed to reduce HDV viremia and block viral entry. Approximately 12 million people worldwide are affected by HDV, underscoring the urgency for effective treatment options. The initial results from SOLSTICE are expected in 2023, marking a significant step forward in addressing this serious health challenge.
Vir Biotechnology will participate in a fireside chat at the Morgan Stanley 20th Annual Global Healthcare Conference on September 13, 2022, at 4:05 p.m. ET. Investors can access a live webcast via the Vir website, which will be archived for 30 days. The company focuses on treating serious infectious diseases using advanced immunologic technologies, with a pipeline aimed at COVID-19, hepatitis B and D, influenza A, and HIV.
Vir Biotechnology reported a net loss of $76.5 million for Q2 2022, significantly down from a net income of $61.8 million in Q2 2021. Total revenues dropped to $40.6 million, influenced by a $397.4 million non-cash charge related to excess sotrovimab supply. Despite this, the company holds over $2.6 billion in cash and equivalents, expected to fund operations for up to five years. Notably, approximately 265,000 sotrovimab doses were delivered in Q2 2022, exceeding initial projections, and the company anticipates important clinical milestones in its COVID-19 and hepatitis programs.
Vir Biotechnology, Inc. (Nasdaq: VIR) announced it will release a corporate update and financial results for Q2 2022 on August 4, 2022, after market close. Investors can access the press release on the company's website. Vir focuses on developing treatments for serious infectious diseases using innovative immunological technologies. Its pipeline includes candidates targeting COVID-19, hepatitis B and D, influenza A, and HIV.